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临床试验/NCT00065065
NCT00065065已完成2 期

A Randomized, Placebo-controlled Trial of Rosiglitazone for Treatment of Ulcerative Colitis

James Lewis13 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2002年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
105
试验地点
13
主要终点
Number of Participants With Improvement of Signs and Symptoms of UC at 12 Weeks

研究概览

简要总结

This is a multicenter, randomized, double-blind, placebo-controlled study evaluating rosiglitazone: 4 mg tablets or placebo tablets administered orally twice daily for 12 weeks. The purpose of the study is to evaluate the efficacy and safety of rosiglitazone in the treatment of mild to moderately active ulcerative colitis. Disease activity will be measured using a standard disease activity index. Calculation of the index requires patients to undergo flexible sigmoidoscopy at the start of the study and at week 12.

详细描述

Ulcerative colitis is a disease characterized by inflammation (the changes that happen when tissues in the body are injured) of all or a portion of the large intestine. There is presently no medical cure for ulcerative colitis, although surgical removal of the colon would cure the disease. Ulcerative colitis is generally treated with medications against diarrhea and infection, medications which suppress the immune system (the body system that protects a person against foreign substances) or with surgery.

It is thought that the chronic inflammation associated with ulcerative colitis may be related to the release of certain chemicals produced by the body. Rosiglitazone has been shown to inhibit the production of some of these chemicals. The active component of rosiglitazone has also been shown to improve colitis in animal models of colitis. The purpose of this study is to evaluate the benefit of the drug for ulcerative colitis by comparing it to placebo.

This is a randomized controlled trial of rosiglitazone versus placebo in patients who have failed to respond to 5-ASA therapy. Participants will be randomized to receive either rosiglitazone 4mg bid or placebo bid twice daily for a total of 12 weeks. Disease activity will be measured using the Disease Activity Index (DAI) at visits 3 through 8. Additional outcomes measured will include histological disease activity (visits 3 and 7) and quality of life using the IBDQ (visits 3 through 8). The principle analyses will be an intent-to-treat analysis to examine the efficacy of rosiglitazone at a dose of 4mg twice daily compared to placebo to achieve a partial or complete response. Additionally, the change in NF-κB activation prior to and following therapy with either placebo or rosiglitazone will be examined using immunohistochemistry techniques.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Rosiglitazone

Experimental

4 mg of rosiglitazone taken twice daily for 12 weeks.

干预措施: Rosiglitazone (Drug)

placebo

Placebo Comparator

Identical in appearance to study drug taken twice daily for 12 weeks.

干预措施: Placebo (Drug)

结局指标

主要结局

Number of Participants With Improvement of Signs and Symptoms of UC at 12 Weeks

时间窗: 12 weeks

Mayo score decrease \>=2 points adjusted for age and smoking status.

次要结局

  • Number of Participants With Clinical Remission at 12 Weeks(12 weeks)
  • Number of Participants With Endoscopic Remission at 12 Weeks(12 weeks)

研究者

发起方
James Lewis
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

James Lewis

Professor of Medicine and Epidemiology

University of Pennsylvania

研究点 (13)

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